Variant report

Variant	nsv880177
Chromosome Location	chr4:144174773-144214082
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:235)
CpG islands
(count:183)
Chromatin interactive
region (count:18)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:235 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:144203086-144203320	HepG2	liver:	n/a	n/a
2	BACH1	chr4:144208366-144208668	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr4:144184095-144184341	H1-hESC	embryonic stem cell:	n/a	n/a
4	CBX3	chr4:144188847-144189225	K562	blood:	n/a	n/a
5	CBX3	chr4:144188882-144189178	K562	blood:	n/a	n/a
6	CTCF	chr4:144208740-144208890	GM12871	blood:	n/a	n/a
7	CTCF	chr4:144208840-144208990	GM12873	blood:	n/a	n/a
8	CTCF	chr4:144208840-144208990	HEK293	kidney:	n/a	n/a
9	CTCF	chr4:144175744-144175843	HepG2	liver:	n/a	chr4:144175769-144175778
10	CTCF	chr4:144194920-144195070	HPAF	blood vessel:	n/a	n/a
11	CTCF	chr4:144175662-144175897	K562	blood:	n/a	chr4:144175769-144175778
12	CTCF	chr4:144175672-144175896	K562	blood:	n/a	chr4:144175769-144175778
13	CTCF	chr4:144208840-144208990	HBMEC	blood vessel:	n/a	n/a
14	CTCF	chr4:144175653-144175869	K562	blood:	n/a	chr4:144175769-144175778
15	CTCF	chr4:144208761-144208971	K562	blood:	n/a	n/a
16	CTCF	chr4:144175320-144175470	HCM	heart:	n/a	n/a
17	CTCF	chr4:144175560-144175710	HA-sp	spinal cord:	n/a	n/a
18	CTCF	chr4:144208770-144209013	K562	blood:	n/a	n/a
19	CTCF	chr4:144208840-144208990	WERI-Rb-1	eye:	n/a	n/a
20	CTCF	chr4:144175698-144175920	H1-hESC	embryonic stem cell:	n/a	chr4:144175769-144175778
21	CTCF	chr4:144208820-144208970	HRPEpiC	eye:	n/a	n/a
22	CTCF	chr4:144208860-144209010	BE2_C	brain:	n/a	n/a
23	CTCF	chr4:144208780-144208930	HMF	breast:	n/a	n/a
24	CTCF	chr4:144175700-144175850	GM12864	blood:	n/a	chr4:144175769-144175778
25	CTCF	chr4:144175587-144175948	H1-hESC	embryonic stem cell:	n/a	chr4:144175769-144175778
26	CTCF	chr4:144175640-144175790	A549	lung:	n/a	chr4:144175769-144175778
27	CTCF	chr4:144208800-144208950	GM12875	blood:	n/a	n/a
28	CTCF	chr4:144213054-144213098	GM20000	blood:	n/a	n/a
29	CTCF	chr4:144208680-144208830	HMEC	breast:	n/a	n/a
30	CTCF	chr4:144208845-144208917	ProgFib	skin:	n/a	n/a
31	CTCF	chr4:144175800-144175950	K562	blood:	n/a	n/a
32	CTCF	chr4:144208580-144208730	GM12864	blood:	n/a	n/a
33	CTCF	chr4:144208860-144209010	GM12864	blood:	n/a	n/a
34	CTCF	chr4:144208800-144208950	GM12873	blood:	n/a	n/a
35	CTCF	chr4:144191500-144191650	NHEK	skin:	n/a	n/a
36	CTCF	chr4:144175720-144175870	K562	blood:	n/a	chr4:144175769-144175778
37	CTCF	chr4:144208820-144208970	HBMEC	blood vessel:	n/a	n/a
38	CTCF	chr4:144208861-144208977	K562	blood:	n/a	n/a
39	CTCF	chr4:144208860-144209010	HFF-Myc	foreskin:	n/a	n/a
40	CTCF	chr4:144208780-144208930	GM12874	blood:	n/a	n/a
41	CTCF	chr4:144197860-144198010	HRPEpiC	eye:	n/a	n/a
42	CTCF	chr4:144175720-144175870	HepG2	liver:	n/a	chr4:144175769-144175778
43	CTCF	chr4:144208880-144209030	HCT-116	colon:	n/a	n/a
44	CTCF	chr4:144208860-144209010	GM12872	blood:	n/a	n/a
45	CTCF	chr4:144175680-144175830	GM12875	blood:	n/a	chr4:144175769-144175778
46	CTCF	chr4:144175682-144175961	H1-hESC	embryonic stem cell:	n/a	chr4:144175769-144175778
47	CTCF	chr4:144208780-144208930	K562	blood:	n/a	n/a
48	CTCF	chr4:144208860-144209010	HepG2	liver:	n/a	n/a
49	CTCF	chr4:144208713-144209028	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr4:144191460-144191610	HCPEpiC	choroid plexus:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:144184682-144184732	ProgFib	skin:	n/a
2	chr4:144208277-144208327	HRE	kidney:	n/a
3	chr4:144207789-144207839	HRPEpiC	eye:	n/a
4	chr4:144184682-144184732	NH-A	brain:	n/a
5	chr4:144184682-144184732	AG04450	lung:	fetal
6	chr4:144208277-144208327	U87	brain:	n/a
7	chr4:144208277-144208327	GM06990	blood:	n/a
8	chr4:144184682-144184732	AG10803	skin:	n/a
9	chr4:144184682-144184732	HL-60	blood:	n/a
10	chr4:144207789-144207839	NHDF-neo	bronchial:	n/a
11	chr4:144207789-144207839	HRE	kidney:	n/a
12	chr4:144207789-144207839	AG04450	lung:	fetal
13	chr4:144207789-144207839	HRCEpiC	kidney:	n/a
14	chr4:144184682-144184732	MCF-7	breast:	n/a
15	chr4:144208277-144208327	HAEpiC	amniotic membrane:	n/a
16	chr4:144207789-144207839	CMK	blood:	n/a
17	chr4:144208277-144208327	GM19239	blood:	n/a
18	chr4:144184682-144184732	U87	brain:	n/a
19	chr4:144208277-144208327	BE2_C	brain:	n/a
20	chr4:144184682-144184732	HepG2	liver:	n/a
21	chr4:144207789-144207839	PrEC	prostate:	n/a
22	chr4:144207789-144207839	Jurkat	blood:	n/a
23	chr4:144184682-144184732	PANC-1	pancreas:	n/a
24	chr4:144208277-144208327	SK-N-SH_RA	brain:	n/a
25	chr4:144207789-144207839	AG09309	skin:	n/a
26	chr4:144208277-144208327	ECC-1	luminal epithelium:	n/a
27	chr4:144207789-144207839	HUVEC	blood vessel:	n/a
28	chr4:144184682-144184732	HCF	heart:	n/a
29	chr4:144208277-144208327	HRCEpiC	kidney:	n/a
30	chr4:144208277-144208327	LNCaP	prostate:	n/a
31	chr4:144208277-144208327	A549	lung:	n/a
32	chr4:144208277-144208327	K562	blood:	n/a
33	chr4:144207789-144207839	GM12892	blood:	n/a
34	chr4:144207789-144207839	HepG2	liver:	n/a
35	chr4:144184682-144184732	Hela-S3	cervix:	n/a
36	chr4:144207789-144207839	ProgFib	skin:	n/a
37	chr4:144207789-144207839	HL-60	blood:	n/a
38	chr4:144184682-144184732	GM06990	blood:	n/a
39	chr4:144208277-144208327	AG09309	skin:	n/a
40	chr4:144208277-144208327	HCT-116	colon:	n/a
41	chr4:144184682-144184732	GM19239	blood:	n/a
42	chr4:144207789-144207839	ECC-1	luminal epithelium:	n/a
43	chr4:144184682-144184732	SK-N-MC	brain:	n/a
44	chr4:144207789-144207839	HEEpiC	esophagus:	n/a
45	chr4:144184682-144184732	PFSK-1	brain:	n/a
46	chr4:144208277-144208327	ovcar-3	ovarian:	n/a
47	chr4:144208277-144208327	GM12878	blood:	n/a
48	chr4:144208277-144208327	HPAEpiC	pulmonary alveolar:	n/a
49	chr4:144184682-144184732	HIPEpiC	eye:	n/a
50	chr4:144208277-144208327	MCF-7	breast:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:144203308..144204917-chr4:144209557..144211230,2	MCF-7	breast:
2	chr4:144200658..144204574-chr4:144257489..144259349,3	MCF-7	breast:
3	chr4:144191423..144193797-chr4:144202159..144203758,2	MCF-7	breast:
4	chr4:144203308..144204917-chr4:144209557..144211230,2	MCF-7	breast:
5	chr4:144105045..144106562-chr4:144200754..144203698,2	MCF-7	breast:
6	chr4:144212380..144214607-chr4:144221526..144224091,2	K562	blood:
7	chr4:142248968..142250827-chr4:144195505..144197291,2	K562	blood:
8	chr4:144209479..144212330-chr4:144213134..144215865,2	K562	blood:
9	chr4:144171110..144173902-chr4:144193418..144195757,2	K562	blood:
10	chr4:144191423..144193797-chr4:144202159..144203758,2	MCF-7	breast:
11	chr4:144213803..144215459-chr4:144216493..144217994,2	K562	blood:
12	chr4:144170301..144172472-chr4:144177727..144180370,2	K562	blood:
13	chr4:144175749..144177348-chr4:144177529..144179744,2	K562	blood:
14	chr4:144174297..144176225-chr4:144302327..144303950,2	K562	blood:
15	chr4:144179114..144181854-chr4:144256791..144259363,2	MCF-7	breast:
16	chr4:144153122..144155090-chr4:144182581..144184458,2	K562	blood:
17	chr4:144175749..144177348-chr4:144177529..144179744,2	K562	blood:
18	chr4:144209479..144212330-chr4:144213134..144215865,2	K562	blood:

(count:1 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GAB1-1	chr4:144207446-144207489	XLOC_003715

No data

Variant related genes	Relation type
ENSG00000250969	TF binding region
ENSG00000250969	CpG island
ENSG00000178972	chromatin interactions
ENSG00000170185	chromatin interactions
ENSG00000250326	chromatin interactions
ENSG00000109458	chromatin interactions

Extended variants
information (count: 1306 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:1306 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs300942	chr4:144174773-144174774	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs570032205	chr4:144174844-144174845	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs190722155	chr4:144174854-144174855	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs12499485	chr4:144174860-144174861	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs182598316	chr4:144174870-144174871	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs144301818	chr4:144174906-144174907	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs111526730	chr4:144174929-144174930	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs185844418	chr4:144174935-144174936	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs534486278	chr4:144174936-144174937	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs536436734	chr4:144174956-144174957	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs554889057	chr4:144175025-144175026	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs570024740	chr4:144175034-144175035	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs537315170	chr4:144175038-144175039	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs189822359	chr4:144175105-144175106	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs143065331	chr4:144175106-144175107	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs113665687	chr4:144175115-144175116	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs147405117	chr4:144175134-144175135	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs574733811	chr4:144175151-144175152	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs542050383	chr4:144175152-144175153	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs187887089	chr4:144175202-144175203	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs530840223	chr4:144175246-144175247	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs571406203	chr4:144175260-144175261	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs376704283	chr4:144175301-144175302	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs115814709	chr4:144175326-144175327	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs74768606	chr4:144175375-144175376	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs553558101	chr4:144175376-144175377	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs75666662	chr4:144175379-144175380	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs546415929	chr4:144175390-144175391	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs193029336	chr4:144175422-144175423	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs184124773	chr4:144175425-144175426	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs73850696	chr4:144175471-144175472	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs569889513	chr4:144175527-144175528	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs557033450	chr4:144175540-144175541	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs575912310	chr4:144175548-144175549	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs188279445	chr4:144175628-144175629	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs202058841	chr4:144175688-144175689	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs139657724	chr4:144175690-144175691	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs570798615	chr4:144175725-144175726	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs192227994	chr4:144175788-144175789	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs553046287	chr4:144175806-144175807	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs574995304	chr4:144175816-144175817	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs78691251	chr4:144175819-144175820	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs557214375	chr4:144175820-144175821	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs575488267	chr4:144175855-144175856	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs72721030	chr4:144175880-144175881	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs75069185	chr4:144175895-144175896	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs10452240	chr4:144175924-144175925	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs569616470	chr4:144176020-144176021	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs561315054	chr4:144176053-144176054	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs528978639	chr4:144176075-144176076	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:72)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	16272173	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Esophageal cancer	21851588	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Olfactory neuroblastoma	18408657	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Mental retardation	17901693	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Myelofibrosis	22110671	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Breast cancer	22048815	CNVD
Autism	22241247	CNVD
Glioblastoma multiforme	22286061	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:266 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:144171800-144174800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr4:144172000-144174800	Enhancers	HMEC	breast
3	chr4:144172200-144174800	Enhancers	NHEK	skin
4	chr4:144172600-144174800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr4:144172600-144176200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr4:144172800-144175600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr4:144172800-144179800	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr4:144172800-144184000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr4:144173600-144175800	Weak transcription	Hela-S3	cervix
10	chr4:144173600-144184000	Weak transcription	HUES48 Cell Line	embryonic stem cell
11	chr4:144173800-144174800	Weak transcription	Sigmoid Colon	Sigmoid Colon
12	chr4:144174400-144177600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr4:144174800-144175800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr4:144174800-144177600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr4:144174800-144177600	Weak transcription	HMEC	breast
16	chr4:144174800-144177600	Weak transcription	NHEK	skin
17	chr4:144175200-144175400	Enhancers	Sigmoid Colon	Sigmoid Colon
18	chr4:144175800-144176000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr4:144175800-144176000	Enhancers	Fetal Stomach	stomach
20	chr4:144175800-144176400	Enhancers	Hela-S3	cervix
21	chr4:144175800-144176600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr4:144176000-144177800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr4:144176200-144176600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
24	chr4:144176400-144177800	Weak transcription	Hela-S3	cervix
25	chr4:144177600-144178200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr4:144177600-144178200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr4:144177600-144178200	Enhancers	HMEC	breast
28	chr4:144177600-144178200	Enhancers	NHEK	skin
29	chr4:144177800-144178200	Enhancers	Hela-S3	cervix
30	chr4:144179800-144180000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
31	chr4:144179800-144180200	Enhancers	iPS-20b Cell Line	embryonic stem cell
32	chr4:144179800-144180600	Enhancers	H9 Cell Line	embryonic stem cell
33	chr4:144180200-144183800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
34	chr4:144180600-144183400	Weak transcription	H9 Cell Line	embryonic stem cell
35	chr4:144181600-144182400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr4:144181800-144182200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr4:144182000-144182400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
38	chr4:144182400-144184000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr4:144182800-144184000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr4:144182800-144184800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr4:144183400-144184400	Enhancers	H9 Cell Line	embryonic stem cell
42	chr4:144183800-144184600	Enhancers	Primary hematopoietic stem cells	blood
43	chr4:144183800-144184800	Enhancers	iPS-20b Cell Line	embryonic stem cell
44	chr4:144184000-144184400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr4:144184000-144184400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr4:144184000-144184400	Enhancers	Primary hematopoietic stem cells short term culture	blood
47	chr4:144184000-144184400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr4:144184000-144184600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
49	chr4:144184000-144184600	Enhancers	Cortex derived primary cultured neurospheres	brain
50	chr4:144184000-144184800	Enhancers	HUES48 Cell Line	embryonic stem cell

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